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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >ANALYSIS OF THE 9-FLUORENYLMETHOXYCARBONYL HYDRAZIDE LABELLING OF NEUTRAL AND SIALIC ACID-CONTAINING OLIGOSACCHARIDES BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY
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ANALYSIS OF THE 9-FLUORENYLMETHOXYCARBONYL HYDRAZIDE LABELLING OF NEUTRAL AND SIALIC ACID-CONTAINING OLIGOSACCHARIDES BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY

机译:反相高效液相色谱法分析中性和唾液酸寡糖的9-氟代甲基氧羰基肼标签

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摘要

Maltoheptaose (M7) and neuraminyllactose (NeuAc-Lac) as models of neutral and sialyl oligosaccharides were derivatized with 9-fluorenylmethoxycarbonyl hydrazide (FMOC hydrazide) at 37 degrees C in acetonitrile-water (50:50) containing 0.5-5% acetic acid without causing any desialylation. The reproducibility of the derivatization of M7 with FMOC-hydrazide was examined and the average relative standard deviation (n=9) was 2.8%. The oligosaccharide FMOC hydrazones were separated on a Cosmosil C-18 column by isocractic elution. The determination limits of M7 and NeuAc-Lac derivatives are at the picomole level for ultraviolet detection and the sub-picomole level for fluorescence detection.
机译:麦芽七糖(M7)和神经氨酸半乳糖(NeuAc-Lac)作为中性和唾液酸低聚糖的模型,在9芴基甲氧基羰基酰肼(FMOC酰肼)在37°C的含0.5-5%乙酸的乙腈-水(50:50)中衍生化,引起任何脱唾液酸化作用。检查了用FMOC-酰肼衍生M7的可重复性,平均相对标准偏差(n = 9)为2.8%。通过等压洗脱在Cosmosil C-18色谱柱上分离寡糖FMOC hydr。 M7和NeuAc-Lac衍生物的测定极限在用于紫外检测的picomole水平和在用于荧光检测的亚picomole水平上。

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